These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


122 related items for PubMed ID: 2576683

  • 1. [Lack of evidence of genetic heterogeneity in a family with adult polycystic kidney (autosomal dominant) distinguished by early onset].
    Guérin P, Lucotte G.
    Nephrologie; 1989; 10(4):201-3. PubMed ID: 2576683
    [Abstract] [Full Text] [Related]

  • 2. A study of genetic linkage heterogeneity in adult polycystic kidney disease.
    Reeders ST, Breuning MH, Ryynanen MA, Wright AF, Davies KE, King AW, Watson ML, Weatherall DJ.
    Trans Assoc Am Physicians; 1986; 99():154-60. PubMed ID: 2885960
    [Abstract] [Full Text] [Related]

  • 3. Clinical and molecular problems of polycystic kidney disease.
    Kucerová M, Zdárský E, Gregor V, Merta M, Kapras J, Dolanská M.
    Czech Med; 1990; 13(4):160-7. PubMed ID: 1981985
    [Abstract] [Full Text] [Related]

  • 4. [Autosomal dominant polycystic kidney and genetic markers of chromosome 16].
    Ferec C, Bourbigot B, Simon P, Whebe B, Treguer H, Hervé JP, Saleun JP, Cledes J.
    Nephrologie; 1990; 11(2):79-82. PubMed ID: 1975432
    [Abstract] [Full Text] [Related]

  • 5. Linkage heterogeneity of autosomal dominant polycystic kidney disease.
    Kimberling WJ, Fain PR, Kenyon JB, Goldgar D, Sujansky E, Gabow PA.
    N Engl J Med; 1988 Oct 06; 319(14):913-8. PubMed ID: 2843768
    [Abstract] [Full Text] [Related]

  • 6. Non-allelic genetic heterogeneity of autosomal dominant polycystic kidney disease?
    Nørby S, Sørensen AW, Boesen P.
    Prog Clin Biol Res; 1989 Oct 06; 305():83-8. PubMed ID: 2762358
    [No Abstract] [Full Text] [Related]

  • 7. [Clinical and molecular problems in polycystic kidneys].
    Kucerová M, Zdárský E, Gregor V, Merta M, Kapras J, Dolanská M.
    Cas Lek Cesk; 1990 Jan 12; 129(2):36-9. PubMed ID: 1970760
    [Abstract] [Full Text] [Related]

  • 8. The molecular genetics of autosomal dominant polycystic kidney disease.
    Reeders ST, Germino GG.
    Semin Nephrol; 1989 Jun 12; 9(2):122-34. PubMed ID: 2672220
    [No Abstract] [Full Text] [Related]

  • 9. [Diagnosis of dominant renal polycystosis in adults by analysis of DNA polymorphism].
    Coto E, Aguado S, Alvarez J, Sanz de Castro S, Arias M, Fernández Toral J, Benavides A, Hernando I, Plasencia A, Herrera J.
    Med Clin (Barc); 1992 Mar 21; 98(11):409-12. PubMed ID: 1349048
    [Abstract] [Full Text] [Related]

  • 10. Characterization of new probes for diagnosis of polycystic kidney disease (PKD1).
    Breuning MH, Verwest A, Ijdo J, Saris JJ, Keith T, Reeders ST, van Ommen GJ, Pearson PL.
    Prog Clin Biol Res; 1989 Mar 21; 305():69-75. PubMed ID: 2569743
    [No Abstract] [Full Text] [Related]

  • 11. Use of 3'HVR genomic probe for presymptomatic diagnosis of adult polycystic kidney disease in northern Italy: comparison of DNA analysis and renal ultrasonographic data.
    del Senno L, de Paoli Vitali E, Zamorani G, Piva R, Hanau S, Buzzoni D, Bernardi F, Storari A, Limone GL, Farinelli A.
    Nephrol Dial Transplant; 1988 Mar 21; 3(6):752-5. PubMed ID: 2906413
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. [Gene diagnosis of adult polycystic kidney disease--linkage analysis between APKD gene and alpha-globin gene 3'HVR].
    Liu G.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1991 Feb 21; 13(1):56-9. PubMed ID: 1678992
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Molecular genetics and polycystic kidney diseases.
    Bachner L, Kaplan JC.
    Adv Nephrol Necker Hosp; 1989 Feb 21; 18():3-18. PubMed ID: 2564249
    [Abstract] [Full Text] [Related]

  • 18. Autosomal dominant polycystic kidney disease and alpha -4.2 thalassemia in a Caucasian family.
    Vinet MC, Dodé C, Pascal O, Monnier N, Rochette J, Bachner L.
    Hum Genet; 1989 Aug 21; 83(1):55-7. PubMed ID: 2767679
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Novel trabecular meshwork inducible glucocorticoid response mutation in an eight-generation juvenile-onset primary open-angle glaucoma pedigree.
    Richards JE, Ritch R, Lichter PR, Rozsa FW, Stringham HM, Caronia RM, Johnson D, Abundo GP, Willcockson J, Downs CA, Thompson DA, Musarella MA, Gupta N, Othman MI, Torrez DM, Herman SB, Wong DJ, Higashi M, Boehnke M.
    Ophthalmology; 1998 Sep 21; 105(9):1698-707. PubMed ID: 9754180
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 7.